Official recall record
EVIS EXERA III Duodenovideoscope (ref 81566)
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-02-03
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
Olympus has updated the reprocessing materials to minimize potential deviations in TJF duodenoscope reprocessing. Olympus is informing users of these changes and is reminding users to closely follow the operation and reprocessing instructions. Users are required to acknowledge reviewing all such materials, which can be accessed through Olympus' education portal.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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